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| Pediatric Tracheostomies For parents and caregivers of children with tracheostomies. Please limit discussion to seeking and sharing of information pertaining to tracheostomy care, medical issues, special needs, disabilities, networking and moral support. |
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#1
05-02-2002, 07:52 AM
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Are you looking for assistance with medical supplies and medicines? What type of financial assistance? We live in North Carolina and I am familiar with some programs for assistance in these areas....but actual money assistance I'm not sure. I could try to find out some more if you let me know your needs.
Just curious is this friend a mom of a trached little one in North Carolina?? Just wondering how close they are to us? Cory
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Parker, 3 Yrs. old., trached at 3 months (Nov. 2000) due to VC paralysis/paresis, DECANNULATED 9/5/03. A great litle guy who loves Hulk, Spiderman and is mommy's true love !!!!! (Page 8 of Aaron's Page) 
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#2
05-02-2002, 07:59 AM
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Ok I guess I'm still sleeping when I went back to the main board I saw you were looking also for medicaid info. I can give you that info. There is a program called CAP-C. (community Alternatives program for children). it is a form of medicaid, however acceptance is not decided on the families income. It's based on the disabilities of the child. There are two levels of care... a hospital level and a skilled level. I could give you more info. on these levels if you'd like. The number is 919-857-4021.
this does aid in pharmacy needs, doc visits, dme supplies and nursing. Hope this helps... cory 
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Parker, 3 Yrs. old., trached at 3 months (Nov. 2000) due to VC paralysis/paresis, DECANNULATED 9/5/03. A great litle guy who loves Hulk, Spiderman and is mommy's true love !!!!! (Page 8 of Aaron's Page)
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